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2013 5
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65 results

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Page 1
Rare and Common Variants in GALNT3 May Affect Bone Mass Independently of Phosphate Metabolism.
Hassan N, Gregson CL, Tang H, van der Kamp M, Leo P, McInerney-Leo AM, Zheng J, Brandi ML, Tang JCY, Fraser W, Stone MD, Grundberg E; Anglo-Australasian Genetics Consortium; Brown MA, Duncan EL, Tobias JH. Hassan N, et al. Among authors: mcinerney leo am. J Bone Miner Res. 2023 May;38(5):678-691. doi: 10.1002/jbmr.4795. Epub 2023 Mar 13. J Bone Miner Res. 2023. PMID: 36824040 Free PMC article.
Genetic testing for familial melanoma.
Primiero CA, Maas EJ, Wallingford CK, Soyer HP, McInerney-Leo AM. Primiero CA, et al. Among authors: mcinerney leo am. Ital J Dermatol Venerol. 2024 Feb;159(1):34-42. doi: 10.23736/S2784-8671.23.07761-7. Epub 2024 Jan 29. Ital J Dermatol Venerol. 2024. PMID: 38287743 Free article.
Unusual suspects in hereditary melanoma: POT1, POLE, BAP1.
Maas EJ, Betz-Stablein B, Aoude LG, Soyer HP, McInerney-Leo AM. Maas EJ, et al. Among authors: mcinerney leo am. Trends Genet. 2022 Dec;38(12):1204-1207. doi: 10.1016/j.tig.2022.06.007. Epub 2022 Jul 7. Trends Genet. 2022. PMID: 35811174
The Future of Precision Prevention for Advanced Melanoma.
Lee KJ, Betz-Stablein B, Stark MS, Janda M, McInerney-Leo AM, Caffery LJ, Gillespie N, Yanes T, Soyer HP. Lee KJ, et al. Among authors: mcinerney leo am. Front Med (Lausanne). 2022 Jan 17;8:818096. doi: 10.3389/fmed.2021.818096. eCollection 2021. Front Med (Lausanne). 2022. PMID: 35111789 Free PMC article.
GOLM1: expanding our understanding of melanoma susceptibility.
Maas EJ, Wallingford CK, DeBortoli E, Smit DJ, Betz-Stablein B, Aoude LG, Stark MS, Sturm RA, Soyer HP, McInerney-Leo AM. Maas EJ, et al. Among authors: mcinerney leo am. J Med Genet. 2023 Sep;60(9):835-837. doi: 10.1136/jmg-2023-109348. Epub 2023 Jul 24. J Med Genet. 2023. PMID: 37487699 No abstract available.
Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice.
Martin EMMA, Enriquez A, Sparrow DB, Humphreys DT, McInerney-Leo AM, Leo PJ, Duncan EL, Iyer KR, Greasby JA, Ip E, Giannoulatou E, Sheng D, Wohler E, Dimartino C, Amiel J, Capri Y, Lehalle D, Mory A, Wilnai Y, Lebenthal Y, Gharavi AG, Krzemień GG, Miklaszewska M, Steiner RD, Raggio C, Blank R, Baris Feldman H, Milo Rasouly H, Sobreira NLM, Jobling R, Gordon CT, Giampietro PF, Dunwoodie SL, Chapman G. Martin EMMA, et al. Among authors: mcinerney leo am. Hum Mol Genet. 2020 Dec 4;29(22):3662-3678. doi: 10.1093/hmg/ddaa258. Hum Mol Genet. 2020. PMID: 33276377 Free PMC article.
NAD Deficiency, Congenital Malformations, and Niacin Supplementation.
Shi H, Enriquez A, Rapadas M, Martin EMMA, Wang R, Moreau J, Lim CK, Szot JO, Ip E, Hughes JN, Sugimoto K, Humphreys DT, McInerney-Leo AM, Leo PJ, Maghzal GJ, Halliday J, Smith J, Colley A, Mark PR, Collins F, Sillence DO, Winlaw DS, Ho JWK, Guillemin GJ, Brown MA, Kikuchi K, Thomas PQ, Stocker R, Giannoulatou E, Chapman G, Duncan EL, Sparrow DB, Dunwoodie SL. Shi H, et al. Among authors: mcinerney leo am. N Engl J Med. 2017 Aug 10;377(6):544-552. doi: 10.1056/NEJMoa1616361. N Engl J Med. 2017. PMID: 28792876 Free article.
Amelanotic/hypopigmented melanoma in a sibship with oculocutaneous albinism.
Maas EJ, Wallingford CK, McGuire JJ, Rutjes C, Smit DJ, Betz-Stablein B, Sturm RA, Soyer HP, McInerney-Leo AM. Maas EJ, et al. Among authors: mcinerney leo am. J Dermatol. 2022 Nov;49(11):1183-1187. doi: 10.1111/1346-8138.16528. Epub 2022 Jul 27. J Dermatol. 2022. PMID: 35894802
65 results